Anti-leukemia effects of ginsenoside monomer: A narrative review of pharmacodynamics study

Background Leukemia is a prevalent disease with high mortality and morbidity rates. Current therapeutic approaches are expensive and have side effects. Objective In this investigation, we reviewed studies that investigated the anticancer effects of ginsenoside derivatives against leukemia and also explained the three main Ginsenoside derivatives (ginsenoside Rg3, Rh2, and Rg1) separately. Methods An extensive search was conducted in Pubmed, Web of Science, and Google Scholar and relevant studies that investigated anticancer effects of ginsenoside derivatives against leukemia cancer were extracted and reviewed. Results Preclinical studies reported that ginsenoside derivatives can induce apoptosis, suppress the proliferation of cancer cells, and induce differentiation and cell cycle arrest in leukemia cells. in addition, it can suppress the chemokine activity and extramedullary infiltration of leukemia cells from bone marrow. using herbal medicine and its derivatives is a promising approach to current health problems. Conclusion This review shows that ginsenoside derivatives can potentially suppress the growth of leukemia cells via various pathways and can be applied as a new natural medicine for future clinical research.


Introduction
Leukemia is a hematologic malignancy that results from the uncontrolled proliferation of leukocytes and originates from myelocytes or lymphocytes.It causes different complications including organ infiltration and pancytopenia, resulting in bleeding due to thrombocytopenia, and increased risk of infection due to leukopenia. 1 Unfortunately, due to the high prevalence and expensive treatments of leukemia, it has high economic burden.On the other hand, Patients with leukemia have poor prognosis and survival.Studies show that the 5-year survival rate of younger patients and one year in older patients is 50 percent. 2There are several challenges with the management and treatment of patients with leukemia.Currently approved drugs for leukemia have side effects and are expensive treatments for example, Bruton tyrosine kinase inhibitors can cause atrial fibrillation arrhythmia in the heart. 3Relapse of disease is another problem in the management of acute leukemia. 4 , 5Thus, investigating novel therapeutic natural products that are safe and efficient in the treatment of leukemia is very necessary.
Ginsenosides are derived from Panax ginseng and contain different.Many studies show that ginsenoside derivatives have anticancer effects against leukemia cancer cells.For instance, in a study by Xia et al., it is shown that ginsenoside Rg3 and Rh2 can induce apoptosis and inhibit the proliferation of human leukemia cells by increasing ROS levels in mitochondria. 6Leukemia stem cells are responsible for the relapsing of acute leukemia, resistance to chemotherapy, and metastasis in patients.Some studies revealed that ginsenoside can target and suppress leukemia stem cells. 2 In this review article, we want to introduce the ginsenoside derivatives and review the preclinical studies that investigated the anticancer effects of ginsenosides against leukemia cancer cells.

Ginseng and its derivatives
Ginseng is the root or rhizome of various perennial herbaceous plants of the genus Panax, which belongs to the family Araliaceae.It has been broadly used as a valuable and popular traditional herbal medicine in East Asian countries mainly China, Korea, and Japan for thousands of years. 7In the past, ginseng was utilized for reinforcement energy and bodily power, enhancement of longevity, and the diminution of stress and exhaustion. 8There are several ginseng species of the genus Panax including Panax ginseng Meyer (Korean ginseng), Panax notoginseng (Chinese ginseng), Panax japonicum (Japanese ginseng), Panax quinquefolius (American ginseng), Panax vietnamensis (Vietnamese ginseng), Panax omeiensis (Omei ginseng), Panax zingiberensis (ginger ginseng), Panax wangianus (narrow-leaved pseudoginseng), and Panax pseudoginseng (Himalayan ginseng). 9Among these, Panax ginseng is one of the most common forms used to treat numerous disorders. 10Ginseng has several beneficial components, including ginsenosides, polysaccharides, polyacetylenes, volatile oils, vitamins, protein, amino acids, and fatty acids. 11 , 12Different types of ginseng are classified based on the growth environment, the cultivation methods (cultivated ginseng, mountain ginseng), and the preparation methods (white ginseng, red ginseng, black ginseng) such as steaming, fermentation, and drying. 13 , 14inseng has numerous pharmacological and therapeutic properties such as anti-stress effects, health betterment, body invigoration, and maintaining and boosting the immune and central nervous systems.ginseng also improves memory and vision actions, alleviates heartbeats, increases intelligence, cognitive ability, and human life span, and is useful in treating common symptoms like tension, insomnia, and headache. 11 , 12 , 15-19Also, it has medicinal applications in the treatment of many diseases including the nervous system, cardiovascular diseases, metabolic diseases, and various types of cancer, and has low adverse effects. 20According to numerous clinical and experimental studies, Ginsenosides have a wide range of effects including anticancer properties against lung, leukemia, breast, and liver cancers, antioxidant, anti-inflammation, anti-apoptosis, anti_proliferative, and anti_metastatis.It also enhances the chemosensitivity of cancer cells, regulates metabolism, and inhibits the migration and invasion of cancer cells ( Figure 1 ).][23][24][25] Additionally, ginsenosides have many other effects in the treatment of neurological disorders including Alzheimer's disease, Parkinson's disease, epilepsy, Huntington's disease, Multiple Sclerosis, and depression. 19 , 26nsenoside: Chemical Structure, Classification, and Pharmacological Effects Ginsenosides are the main bioactive ingredient of ginseng and are the type of triterpene saponins.16 Until now, more than 180 types of ginsenosides have been obtained from Panax species and their pharmacological effects have been determined.27 The basic structure of ginsenosides is similar.All of them contain 30 carbon atoms and are composed of steroid nuclei having 17 carbon atoms arranged in four rings backbone (Aglycon moiety) ( Figure 2 ).The type, position, and number of diverse sugar molecules (e.g., glucose, rhamnose, xylose, and arabinose) connected at C-3, C-6, and C_20 positions of the rings (Glycoside moiety) variate the ginsenosides derivatives and influences on biological as well as pharmacological effects of ginsenosides. 11 , 28 According to the positioning of hydroxyl (OH) on carbon 20 (C20), the dammarane group of ginsenosides (PPD and PPT types) has two major categories; 20(S) and 20(R) epimers include 20(S)-protopanaxadiol (PPD) and 20(S)protopanaxatriol (PPT), 20(R)-protopanaxadiol (PPD) and 20(R)protopanaxatriol (PPT) types ( Figure 3 ).29 The PPD category is determined by the sugar molecule connection at C-3 and/or C-20 position, and the PPT category is identified by the sugar molecule connection at C-6 and/or C-20 position.16 , 30 PPT-and PPD-type ginsenosides are plentiful in Panax ginseng, P. quinquefolius, and P. notoginseng; and P. japonicasi, while P. vietnamensis contains OT-type ginsenosides.also, OA-type ginsenoside is abundant in other species of ginseng (P.zingiberensi, P. stipuleanatus, P. bipinnatifidus, and P. sokpayensis).9 So far, among ginsenosides obtained from different ginseng plants, Four PPD-type ginsenosides (Rb1, Rb2, Rc, and Rd) and two PPT-type ginsenosides (Re and Rg1) responsible for almost 90% of the total ginsenosides and are considered as the main ginsenosides.9 , 16 Due to differences in the type and amount of ginsenosides in various Panax species, there is diversity in their pharmacological activities.9

Ginsenoside Rh2
The pharmacological effects of Ginsenoside Rh2 (GR2), a member of the Ginsenosides family, have been observed in various cancer types, including leukemia cells.GRh2 can cause cell cycle arrest in the G1 phase via Retinoblastoma protein phosphorylation reduction and transcription factor translocation. [31][32][33] GRh2 is a potential Histone deacetylase inhibitor for leukemia treatment as it effectively induces cell cycle arrest and apoptosis, increased Histone acetyltransferase (HAT) activity and histone acetylation, and can inhibit the growth of human leukemia cells. 34 , 35iaoru Wang conducted a study to investigate the therapeutic potential of GRh2 in pediatric leukemia.They reported that GRh2 can suppress the Bcl-2 expression by modulating miR-21 which leads to a decrease in cell viability and increase in apoptosis.These results suggest that GRh2 could be a promising treatment option for pediatric leukemia. 36GRh2 was found to be capable of inducing both apoptosis and autophagy in ALL cells specifically without advert effects on normal blood cells.However, it was also found that autophagy plays a protective role in GRh2induced apoptosis.In other words, the autophagy process helps the cells to resist GRh2-induced apoptosis.The researchers discovered that inhibiting autophagy can make ALL cells more sensitive to GRh2-induced apoptosis.In conclusion, inhibition of autophagy can sensitize ALL cells towards GRh2 and make it a more effective anti-cancer agent for ALL therapy. 37Also, GRh2 is considered a chemotherapeutic agent for leukemia therapy by inducing apoptosis through the mitochondrial pathway including mitochondrial depolarization, cytochrome complex release, and activation of caspase-9 and caspase-3 in acute leukemia cells. 38Rh2 exhibits immune regulation and anti-tumor effects in T-cell acute lymphoblastic leukemia (T-ALL) by blocking the Phosphatidylinositol 3-kinase / Mammalian target of rapamycin (PI3K/Akt/mTOR) signaling pathway, enhancing immunity in the spleen, promoting intestinal homeostasis, and altering the composition of gut microbiota, indicating that it may have the potential for the prevention and treatment of T-ALL. 39Furthermore, another   40 Another study showed that GRh2 decreased NB4 cell viability in a dose-and time-dependent manner and induced apoptosis, cell cycle arrest, and caspase activation.GRh2 also upregulated Tumor necrosis factor alpha (TNF-α) expression and inhibited Akt phosphorylation, leading to Promyelocytic leukemia/Retinoic acid receptor alpha (PML/PML-RARA) degradation, PML nuclear bodies formation, and activation of the downstream p53 pathway in NB4 cells.The study concluded that GRh2 induces caspasedependent PML-RARA degradation and apoptosis through the Akt/Bax/caspase9 and TNF-α /caspase8 pathways. 41GRh2 induces cell death via apoptosis and autophagy in AML and CML cells, with a stronger apoptotic effect in K562 cells.Autophagy plays a protective role against apoptosis, suggesting that combining GRh2 with autophagy inhibitors may have therapeutic potential for AML and CML. 42GRh2 can slow downregulation of the growth of HL-60 leukemia cells by preventing them from progressing through the G1 phase of the cell cycle and causing them to differentiate.This effect may be due to the increased expression of cyclin-dependent kinase inhibitor 1 (p21CIP1/WAF1), which inhibits the activity of cyclin-dependent kinases CDK2, CDK4, and CDK6. 43o summarize, it can be briefly stated that multiple studies have demonstrated the remarkable anti-cancer capabilities of GRh2 with minimal negative consequences.GRh2 can induce apoptosis and inhibit the growth of cancer cells by increasing the production of TNF-α.Additionally, it can cause G1 cell cycle arrest and differentiation in leukemia cells by elevating Transforming growth factor-beta (TGF-β) levels.Due to its various mechanisms of action such as cell cycle arrest, Histone deacetylase inhibition, upregulation of p21CIP1/WAF1, and downregulation of CDK2, CDK4, and CDK6 activities, GRh2 is being increasingly recognized as a highly effective and hopeful treatment for leukemia with significant anti-tumor properties and limited adverse effects ( Table 1 ).

Ginsenoside Rg3
Ginsenoside Rg3 (GRg3) is a type of ginsenoside found in high quantities.5][46][47] GRg3 has been found to have anti-cancer effects in many types of cancer.In short, it induces apoptosis, arrests the cell cycle, inhibits the growth, proliferation, and metastasis of cancer cells, and prevents angiogenesis against cancer cells. 48ased on previous studies, GRg3 induces apoptosis in leukemia by downregulating Phosphatidylinositol 3-kinase (PI3K/Akt) family proteins. 49Also, GRg3 has been found to lower vascular endothelial growth factor (VEGF) expression in acute leukemia patients by deactivating the PI3K/Akt and extracellular signal-regulated kinase ½ (ERK1/2) pathways. 50In another research, GRg3 triggered programmed cell death in Jurkat cells and resulted in the formation of condensed nuclei and apoptotic bodies.It also increases the expression levels of apoptosis-associated proteins, such as caspase-3 and -9, and reduces the expression of VEGF.It can inhibit cell proliferation by inducing excessive mitochondrial reactive oxygen species (ROS), which results in a reduction in mitochondrial membrane potential. 51Rg3 can be potentially used as a supplementary treatment for leukemia.Multidrug resistance (MDR) poses a major obstacle to the effectiveness of current cytotoxic drugs in achieving optimal outcomes for cancer treatment.GRg3 has been shown to enhance the effects of anticancer agents in MDR cells by modulating efflux-mediated drug accumulation defects.Specifically, 20(S)-Rg3 exhibits the most potent inhibitory activity on MDR by inhibiting the drug efflux pump and increasing drug accumulation in MDR cells.Overall, GRg3 has the potential to enhance the effectiveness of chemotherapy in cancer treatment. 52In a separate study, the co-administration of GRg3 and doxorubicin using a co-loaded biomimetic nanosystem resulted in increased tumor immunogenicity and improved immune system response, suggesting its potential as an adjuvant treatment for AML. 53n summary, GRg3 has demonstrated remarkable anti-tumor effects in various studies with minimal side effects.Moreover, it improves the therapeutic results and efficacy of chemotherapy and radiotherapy by affecting multiple antioxidant, anti-inflammatory, and immune signaling pathways.Additionally, it inhibits tumor cell proliferation and neovascularization, promotes tumor cell apoptosis, and reverses tumor chemoresistance.In light of its demonstrated remarkable anti-tumor functions, minimal side effects, and multiple mechanisms of action, GRg3 is increasingly recognized as a promising and effective antitumor agent in the field of oncology ( Table 2 ).

Ginsenoside Rg1
Another ginseng derivative that is used for the treatment of leukemia is Ginsenoside Rg1 (GRg1).Some studies indicated that Rg1 can induce senescence markers such as beta-galactosidase in leukemia cells. 2 , 54 , 55 Yan et al. performed a study to investigate the anticancer effects of GRg1 on KG1 α leukemia cells.they isolated the CD34 + /CD38-leukemia stem cells from the KG1 α cell line and divided them into control and GRg1 groups.Results show that Rg1 can significantly reduce the proliferation of stem cells compared to the control group.In addition, there were more cancer stem cells in the G0/G1 phase of the cell cycle and also fewer cancer stem cells in the G2/M and S phase of the cell cycle in the GRg1 group compared with the control group.Finally, they concluded that GRg1 induced the expression of beta-galactosidase as a senescence marker and suppressed the Sirtuin 1 and tuberous sclerosis complex 2 (TSC2) gene expression.The sirtuin 1 gene is responsible for cell proliferation and senescence and interaction with TSC2.It is shown that overexpression of Sirtuin 1 is related to resistance to treatment of leukemia. 2Induction of senescence in leukemia stem cells by GRg1 was observed in another study.It could increase the p16INK4a expression that has antitumor activity and also decrease the hTERT (Telomerase reverse transcriptase) expression. 55n 2014 Li et al. designed a study to investigate the anticancer activity of GRg1 against acute myeloid leukemia.They found that the proliferation of leukemia cancer cells is suppressed after treatment of cells with GRg1 in a dose and time-dependent manner.The effects of GRg1 on apoptosis-related genes are considerable.It was shown that GRg1 can induce apoptosis by upregulating the

Table 1
Anti-cancer effect of GRh2 on leukemia cell lines

Aim of Study
Results References To determine the potential of GRh2 as an HDAC inhibitor for the treatment of leukemia -GRh2 may be a useful HDAC inhibitor for treating leukemia, as it has been shown to halt cell cycle progression, promote apoptosis, reduce cell proliferation proteins, increase HAT activity and histone acetylation, and inhibit the growth of leukemia tumors Liu, Z.H et al.
(2015) 35 To investigate the molecular mechanisms of cell death induced by GRh2 in ALL cells -GRh2 can effectively induce apoptosis and autophagy in ALL cells without affecting normal blood cells, and inhibiting autophagy can enhance the potency of GRh2 as an anticancer agent for ALL therapy by sensitizing ALL cells to its effects Xia, T et al.
(2016) 37 To inspect GRh2 anti-tumor effects Related to both the immune system and the gut microbiota -In T-ALL mice, Bacteroidetes, Verrucomicrobia, Akkermansia, Lactobacillus, and Lachnospiraceae showed positive correlations with immune parameters and gut barrier functions, while Firmicutes, Proteobacteria, Parabacteroides, and Alistipes showed negative correlations Xia T, et al.
(2020) 39 To investigate the effects of GRh2 on the proliferation, cell cycle regulation, and differentiation of human leukemia HL-60 cells -GRh2 inhibits the proliferation of human leukemia HL-60 cells via G1 phase cell cycle arrest and induces differentiation, possibly through up-regulation of p21CIP1/WAF1 and down-regulation of CDK2, 4, and 6 To evaluate the impact of GRh2 on human acute T lymphoblastic leukemia Jurkat cells and the underlying mechanism -GRh2 inhibited Jurkat cell proliferation in a dose-time dependent manner, induced apoptosis and cell cycle block in the G0/G1 phase, and promoted the expression of BAX and Caspase-3 while inhibiting the expression of BCL-2, Cyclin D1, and p-AKT, with PI3K inhibitor LY294002 enhancing these effects Nie L, Peng HM. (2019) 58 To analyze the effect of GRh2 on leukemia

Table 2
Anti-cancer effect of GRg3 on leukemia cell lines

Aim of Study Results References
To explore the effect of 20-(s)-GRg3 on apoptosis in human leukemic U937 and HL-60 cells and the underlying mechanism.
-20-(S)-GRg3 induced apoptosis in both U937 and HL-60 cells in a dose-dependent manner and this effect was attributed to the activation of caspase-3 and the downregulation of Bcl-2 expression.
Xiao-Min et al.
(2014) 49 Investigation of the anti-angiogenic effects of Rg3 in patients with acute leukemia.
-Rg3 inhibited the expression of HIF-1 α and VEGF in BMSCs through the downregulation of -GRh2 and GRg3 inhibited cell growth and induced apoptosis, but GRh2 had greater cytotoxicity than GRg3.
-The expression levels of apoptosis-associated proteins were significantly increased in Jurkat cells treated with GRh2 compared to GRg3.

Ting Xia et al. (2017) 51
To determine whether an interaction between the two compounds would allow lower concentrations to be used clinically to modulate drug resistance.
-20S-Rg3 may be used as a Vp synergize or as a promising alternative to Vp in the chemosensitization of multidrug-resistant acute myeloid leukemia, with far fewer side effects.
Sung Su et al. (2014) 52 explain the impacts of ginsenosides in non-neoplastic conditions and neoplastic conditions -The viability of human leukemic cells is reduced and apoptosis is induced by 20-(S)-GRg3 through the increased activity of caspase-3 and caspase-9.

Ghafouri-Fard et al. (2022) 63
To introduce a novel biomimetic nanosystem that can co-load doxorubicin and ginsenoside and be used for chemoimmunotherapy of acute myeloid leukemia -Rg3 was found to enhance tumor sensitivity to DOX, activate the anti-tumor immune response, and effectively combat leukemia cells in the bone marrow. 53 explore how GRg3 affects HIF-1 α and VEGF levels in bone marrow stromal cells (BMSCs) in acute leukemia, and identify the underlying mechanism.

Mo Chen et al. (2022)
-Rg3 inhibits HIF-1 α and VEGF expression in leukemia BMSCs and downregulates PI3K/Akt and MAPK pathways, suggesting an anti-angiogenesis role in acute leukemia bone marrow.Inhibitory effects of GRg1 on the proliferation of leukemia stem cells through SIRT1/TSC2 signaling pathway -After treatment with GRg1, leukemia cells in the G2/M and S phases of replications were reduced significantly whereas cells in the G0/G1 phase of replication were elevated -Mixed colony-forming unit and beta-galactosidase (senescence markers) were increased significantly -GRg1 can inhibit proliferation and induce senescence markers in leukemia stem cells through activation of the SIRT1 TSC2 signaling pathway Bax and caspase 3 proteins and reducing the expression of EpoR (a key gene in oncogenic signaling pathways).It inactivates the JAK2/STAT5 signaling pathway which has important effects on cell proliferation, survival, and apoptosis.GRg1 toxicity wasn't observed in less than 100μM concentration ( Table 3 ). 56

Other ginsenoside derivatives
Other forms of ginsenosides are also discussed in studies.Compound k (CK) is another ginsenoside derivative that has been used for the suppression of leukemia cells.CK can potentially target the cancer cells by different mechanisms.Telomerase has an important role in the pathogenesis of cancer cells and is activated in most types of cancer cells.CK inhibits the telomerase function and causes apoptosis and cell cycle arrest in the G1 phase. 70Another study shows that It can induce apoptosis in HL-60 leukemia cells by activation of caspase-3 and caspase-9 enzymes. 71 , 72In 2013, Chen et al. investigated the anti-leukemic activity of CK on pediatric myeloid leukemia cells.They assessed the proliferation, apoptosis, cell viability, and cell cycle of cancer cells after the application of CK. Results show the inhibitory effect of CK on the growth and proliferation of myeloid leukemia cells in a time and dosedependent manner.CK induces apoptosis and cell cycle arrest and also suppresses the synthesis of DNA in cancer cells.They concluded that CK can be a potential natural medicine for the improvement of pediatric acute myeloid leukemia. 73n another study by Ma et al., they reported that ginsenoside Rk3 can inhibit the extramedullary infiltration of leukemia cells.Researchers measured the expression of mir-3677-5p and CXCR4 and investigated the correlation of them using Rk3.It was shown that overexpression of mir-3677-5p inhibits the invasion, migration, and proliferation of leukemia cells.In contrast, the patients with extramedullary infiltration of leukemia have higher expression of CXCR4.In the Rk3 group, the expression of mir-3677-5p was significantly higher than in the control group whereas the expression of CXCR4 was decreased compared to the control group after treatment with Rk3. 68Ginsenoside Rh1 is another ginsenoside derivative with anti-inflammatory and antiallergic properties.Choi et al. found that Rh1 can inhibit the migration and invasion of THP-1 cells and reduce the expression of Monocyte chemoattractant protein 1(MCP-1) and CCR2 (chemokine receptor).MCP-1 is a chemokine that is increased in untreated patients with AML. 69 , 74he combination of ginsenoside derivatives with chemotherapeutic medications is also investigated for the treatment of leukemia.For example, Qi et al. reported the anticancer effects of ginsenoside CK combined with cytarabine for the treatment of acute myeloid leukemia cells.It was shown that CK and cytarabine synergistically inhibit the proliferation of cancer cells, increase cytotoxicity, induce apoptosis, and also cause DNA damage in leukemia cells. 5In another investigation, Chen et al. used GRg3 with doxorubicin for the treatment of AML.They loaded these drugs into a platelet membrane-based nano-system and investigated their efficacy in the suppression of leukemia cells.They reported that the sensitivity of leukemia cells to doxorubicin increases when it is used in combination with GRg3.In addition, it was shown that a combination of GRg3 and doxorubicin can potentially activate T cells against leukemia cells.GRg3 had a synergistic effect on the immunogenic death of cancer cells when used with doxorubicin. 75On the other hand, some studies reported that the application of GRg1 along with doxorubicin decreases the side effects of chemotherapy such as doxorubicin-induced cardiotoxicity. 76A meta-analysis that analyzed the results of 18 clinical trials showed that GRg3 improves chemotherapy-induced cytopenia and recommended GRg3 for myelosuppression patients. 77Besides doxorubicin, it was shown that GRg3 increases the sensitivity of leukemia cells to the vincristine. 78n conclusion, using agents that potentiate the anticancer activity of chemotherapeutic drugs, especially in chemotherapy resistance-cancers, and decrease the adverse effects of chemotherapy are beneficial for cancer patients.Further research is needed to illustrate the efficacy of ginsenoside derivatives for the promotion of chemotherapeutic medications efficacy and preventing their side effects ( Figure 4 ).

Conclusion
In this study, we reviewed the anticancer potential of ginsenosides against leukemia cancer cells.Ginsenosides induce apoptosis and cell cycle arrest, suppress the proliferation of cancer cells, induce senescence markers, and suppress the leukemia cancer cells via different signaling pathways including the JAK2/STAT5 signaling pathway.However, the results of preclinical studies are promising, more studies especially clinical trial studies are required to investigate the safety and efficacy of ginsenosides on leukemia patients.

Declaration of competing interest
There isn't any competing interest in this research.

Funding
In this research, we didn't use any funding.

Figure 1 .
Figure 1.Potential biological and pharmacological activities of ginsenoside

Figure 2 .
Figure 2. Ginsenosides Structures study demonstrated that GRh2 can effectively inhibit the growth of T-ALL cells by inducing apoptosis and autophagy and blocking the PI3K/Akt/mTOR signaling pathway.The study showed that GRh2 could reduce T-ALL progression.These results suggest that GRh2 may have therapeutic potential for T-ALL treatment.40Another study showed that GRh2 decreased NB4 cell viability in a dose-and time-dependent manner and induced apoptosis, cell cycle arrest, and caspase activation.GRh2 also upregulated

KG1 α cells -
Rh2 is the most effective ginsenoside on the growth of KG1 α cells -GRh2 had the lowest Half-maximal inhibitory concentration (IC50) compared to Rb1, Rg1 and cytarabine You Z, et al. (2014)59 To investigate the effect of GRh2 on inducing apoptosis of human leukemia K562 cells -GRh2 inhibited cell proliferation, induced apoptosis and autophagy, and activated p-p38, which could be weakened by an autophagy inhibitor Liu XX, et al. (2017)60 To inspect how GRh2 can inhibit human leukemia cells and understand how it works in terms of autophagy and apoptosis -Ginsenoside Rh 2 inhibits human leukemia cell growth in vivo through the regulation of autophagy and apoptosis via the HDAC6 and Heat shock protein 90 pathwaysLiu ZH, et al.  (2016) 61 To investigate the effects of GRh2 on cell proliferation, HDAC1 and HDAC2 activity, and expression of cyclin in human erythroleukemia K562 cells -GRh2 inhibited the proliferation of K562 cells, induced cell cycle arrest, and apoptosis, and reduced HDAC activity through downregulating cyclin D1 and activating cyclin-dependent kinase inhibitor 2A (p16INK4A) and p21 Xia J, et al. (2014)62 Akt and ERK1/2 phosphorylation.Dongfeng Zeng et al. (2014)50 Investigation of the anticancer properties of GRh2 and GRg3 in Jurkat cells.

Tang et al. (2020) 2
Induction of senescence in leukemia stem cells by GRg1 through the effect on p16INK4a and hTERT gene expression -GRg1 can induce Senescence in leukemia stem cells by overexpression of p16INK4a and suppression of hTERT expression Tang et al. (2021)55 Effects of GRg1 on K562 leukemia cell line -After treatment with GRg1, the senescence-related proteins, and beta-galactosidase were increased.Also, GRg1 can inhibit proliferation and colony formation and cause shortened telomere length.It can also alter the morphology of cancer cells by increasing mitochondria size and lysosomes number Liu et al. (2012) 65 Anti-cancer activity of GRg1 on K562 leukemia cancer cells -Induction of apoptosis through upregulation of Bax, CPAPR protein, caspase 3, and suppression of Bcl-2, and AG490 -Inhibition of the JAK2/STAT5 pathway and suppression of EpoR expression Li et al. (2014) 56 Discovering the effects of GRg1 on inducing senescence in K562 leukemia cells by -Inhibition of K562 cell proliferation and cell cycle arrest in the G2/M phase -Upregulation of senescence-related genes (P16, P21, P53, and Rb) Cai et al. (2012) 54 Investigation of ginsenoside CK effects against acute myeloid leukemia -Induction of apoptosis and G1 cell cycle arrest -Upregulation of TET2 gene expression -Downregulation of CSF-1, KIT, BCL2, MYC, and DNMT3A gene expression -In conclusion, CK is a safe and efficient agent against myeloid leukemia cells Hou et al. (2022) 66 Synergistic activity of ginsenoside CK and cytarabine on acute myeloid leukemia cells -The cytotoxicity, DNA damage, and apoptosis induced by cytarabine are promoted by ginsenoside CK Qi et al. (2020) 5 Investigation of CK effects on human leukemia cells -Induction of apoptosis in leukemia via caspase activation -Inhibition of leukemia cell viability Cho et al. (2009) 67 Investigation of ginsenoside Rk3 effects on extramedullary infiltration of AML -Inhibition of extramedullary infiltration of cancer cells -Suppression of invasion, migration, and proliferation of SHI-1 leukemia cells -Increase the expression of mir-3677-5p Ma et al. (2022) 68 Anticancer effects of ginsenoside Rh1 against acute monocytic leukemia -Decrease the expression of MCP1 and CCR2 in monocytes -Inhibition of invasion and migration of THP-1 leukemia cell line through suppression of MAPK pathway -Cytotoxicity of GRh2 against leukemia cells wasn't seen in 50μM concentration Choi et al. (2011)69

Figure 4 .
Figure 4. Mechanism of action of ginsenoside derivatives

Table 3
Anticancer effects of GRg1 on leukemia cancer cell lines